Pesce Giampaola, Auricchio Renata, Bagnasco Marcello, Saverino Daniele
1 Autoimmunity Unit, Department of Internal Medicine, University of Genova , Genova, Italy .
Genet Test Mol Biomarkers. 2014 Jan;18(1):8-11. doi: 10.1089/gtmb.2013.0350. Epub 2013 Oct 19.
To evaluate the levels of soluble CTLA-4 (sCTLA-4) in sera of celiac disease (CD) patients with overlapping autoimmune diseases (OAD; diabetes mellitus, autoimmune thyroid diseases, inflammatory bowel diseases, and autoimmune polyendocrine syndromes).
Sera from Italian patients with CD were obtained and enzyme-linked immunosorbent assay was used to measure sCTLA-4.
Consistently high serum sCTLA-4 levels were observed in CD (13.20 ng/mL, p<0.0001) and OAD (19.48 ng/mL, p<0.0001) compared to normal controls. A significant increase in the level of serum sCTLA-4 was observed in OAD (p=0.0273) compared to CD alone. At variance, no significant difference in the sCTLA-4 levels was observed when single OAD were compared.
The present study shows for the first time a statistically significant increase of serum sCTLA-4 levels in CD patients with associated autoimmune disease (namely, CD and OAD) versus patients with CD alone. Previously, the potential genetic associations of several CTLA-4 polymorphisms to susceptibility to autoimmune diseases have been described, although the relationship between CTLA-4 polymorphisms and the ability to produce the soluble form is not fully clarified. CTLA-4 is a strong actor in the adaptive response: our data give supportive evidence of the common background of autoimmune diseases.
评估患有重叠自身免疫性疾病(OAD,即糖尿病、自身免疫性甲状腺疾病、炎症性肠病和自身免疫性多内分泌综合征)的乳糜泻(CD)患者血清中可溶性细胞毒性T淋巴细胞相关抗原4(sCTLA-4)的水平。
获取意大利CD患者的血清,采用酶联免疫吸附测定法测量sCTLA-4。
与正常对照组相比,CD患者(13.20 ng/mL,p<0.0001)和OAD患者(19.48 ng/mL,p<0.0001)血清sCTLA-4水平持续升高。与单纯CD患者相比,OAD患者血清sCTLA-4水平显著升高(p=0.0273)。不同的是,比较单一OAD时,sCTLA-4水平未观察到显著差异。
本研究首次表明,与单纯CD患者相比,患有相关自身免疫性疾病(即CD和OAD)的CD患者血清sCTLA-4水平有统计学意义的显著升高。此前,已描述了几种CTLA-4多态性与自身免疫性疾病易感性的潜在遗传关联,尽管CTLA-4多态性与产生可溶性形式的能力之间的关系尚未完全阐明。CTLA-4在适应性反应中起重要作用:我们的数据为自身免疫性疾病的共同背景提供了支持性证据。